Evidence map›Paper›PMID 32923621›Full record

ArticleScience advances2020

Sustained release of a GLP-1 and FGF21 dual agonist from an injectable depot protects mice from obesity and hyperglycemia.

C A Gilroy, M E Capozzi, A K Varanko, J Tong, D A D'Alessio, J E Campbell, A Chilkoti

Open access · goldAbstract read
In one paragraph

Article in Science advances, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed, 2 pooled it
3.3field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

43 citing papers in PubMed, 2 syntheses or guidelines pooled it, 76 citations in OpenAlex.

  1. Pooled it
  2. Liver Brain Interactions: Focus on FGF21 a Systematic Review.International journal of molecular sciences · 2022
    Pooled it
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Hypothalamus-liver talks: whispers in the language of metabolism.Reviews in endocrine & metabolic disorders · 2026
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. FGF21 analogue PF-05231023 on alcohol consumption and neuronal activity in the nucleus accumbens.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Article
  15. Review
  16. Article
  17. Article
  18. GLP-1-Mediated Pregnancy and Neonatal Complications in Mice.Journal of developmental biology · 2025
    Article
  19. Article
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

C A GilroyDepartment of Biomedical Engineering, Duke University, Durham, NC 27708, USA.ORCID 0000-0001-8225-6314
M E CapozziDuke Molecular Physiology Institute, Duke University, Durham, NC 27701, USA.ORCID 0000-0002-7587-0663
A K VarankoDepartment of Biomedical Engineering, Duke University, Durham, NC 27708, USA.
J TongDuke Molecular Physiology Institute, Duke University, Durham, NC 27701, USA.ORCID 0000-0002-5614-3671
D A D'AlessioDuke Molecular Physiology Institute, Duke University, Durham, NC 27701, USA.
J E CampbellDuke Molecular Physiology Institute, Duke University, Durham, NC 27701, USA.ORCID 0000-0003-4358-6331
A ChilkotiDepartment of Biomedical Engineering, Duke University, Durham, NC 27708, USA.ORCID 0000-0002-1569-2228
Duke University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is great interest in identifying a glucagon-like peptide-1 (GLP-1)-based combination therapy that will more effectively promote weight loss in patients with type 2 diabetes. Fibroblast growth factor 21 (FGF21) is a compelling yet previously unexplored drug candidate to combine with GLP-1 due to its thermogenic and insulin-sensitizing effects. Here, we describe the development of a biologic that fuses GLP-1 to FGF21 with an elastin-like polypeptide linker that acts as a sustained release module with zero-order drug release. We show that once-weekly dual-agonist treatment of diabetic mice results in potent weight-reducing effects and enhanced glycemic control that are not observed with either agonist alone. Furthermore, the dual-agonist formulation has superior efficacy compared to a GLP-1/FGF21 mixture, demonstrating the utility of combining two structurally distinct peptides into one multifunctional molecule. We anticipate that these results will spur further investigation into GLP-1/FGF21 multiagonism for the treatment of metabolic disease.

Indexed as

Diabetes Mellitus, ExperimentalDiabetes Mellitus, Type 2HyperglycemiaAnimalsDelayed-Action PreparationsFibroblast Growth FactorsGlucagon-Like Peptide 1Glucagon-Like Peptide-1 Receptor AgonistsHumansMiceObesityPeptidesDelayed-Action Preparationsfibroblast growth factor 21Fibroblast Growth FactorsGlucagon-Like Peptide 1Glucagon-Like Peptide-1 Receptor AgonistsPeptides

Identifiers

PMID32923621
PMCPMC7449677
OpenAlexW3080167769

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.